Compare the 1 manufacturers holding an active US Drug Master File for Histrelin API, with DMF numbers and filing years from the FDA's quarterly DMF list.
Directory listing last reviewed October 2026.
1 manufacturer holds an active Type II Drug Master File for HistrelinAPI, taken from the FDA's quarterly DMF list. A DMF lets a drug applicant reference the maker's manufacturing data. It is not an FDA approval. Check each manufacturer against the FDA import alert lists before ordering.
Request Histrelin API quotes| Manufacturer | Location | US DMF | Filed |
|---|---|---|---|
| Bachem Holding AG | Switzerland / USA | 16997 | 2003 |
Request API quotes from several manufacturers at once. Compare other molecules on the peptide API manufacturers index.